Prosthetic valve with tissue anchors configured to exert opposing clamping forces on native valve tissue

ABSTRACT

A prosthetic valve configured for implantation within a native valve may be provided. The prosthetic valve may include an expandable valve body having an inner lumen extending along a longitudinal axis of the valve body. The prosthetic valve may additionally include a plurality of ventricular tissue anchors configured to extend from the valve body to ventricular anchor distal ends, as well as a plurality of atrial tissue anchors configured to extend from the valve body to atrial anchor distal ends. Each atrial tissue anchor may include a rigid portion, and a flexible portion situated between a distal end of the rigid portion and the atrial anchor distal end. The ventricular anchor distal end of a ventricular tissue anchor and the distal end of the rigid portion of an atrial tissue anchor may be configured to be equidistant from the longitudinal axis of the valve body.

CROSS-REFERENCE TO RELATED APPLICATION

This application claims priority from U.S. Provisional Patent Application No. 62/560,384, filed Sep. 19, 2017, which is hereby incorporated by reference in its entirety.

TECHNICAL FIELD

This disclosure relates generally to prosthetic valves and delivery systems for prosthetic valves. More specifically, this disclosure relates to prosthetic heart valves and methods thereof.

BACKGROUND

The native heart valves (the tricuspid valve, pulmonary valve, mitral valve, and aortic valve) play an important role in regulating flow of blood through the cardiovascular system. However, the native heart valves may become damaged or impaired due to, for example, cardiovascular diseases, infections, or congenital malformations, thus limiting the ability of the native heart valves to regulate blood flow. This deficiency may result in reduced cardiovascular function or even death.

To treat these conditions, prosthetic heart valves may be implanted at or near the site of a damaged or impaired native valve. A prosthetic heart valve may assist or replace the functionality of an impaired native valve, leading to better regulation of blood flow and improved cardiovascular function. However, many existing prosthetic heart valves require implantation via an open heart procedure, which is highly-invasive and may cause life-threatening complications. Other prosthetic valves may be collapsed within a prosthetic valve delivery system and advanced into the heart, at which point the prosthetic valve may be removed from the delivery system and expanded at the native valve site. However, many of these prosthetic valves are large in size and therefore difficult to deliver into the heart without causing damage to healthy tissue along the implantation route. In addition, once these prosthetic valves are situated within the heart, they may be difficult to securely implant at the native valve site due to their complex structure and the limited maneuverability of existing prosthetic valve delivery systems within the heart. Moreover, many prosthetic valves are so large that they may protrude several centimeters into surrounding heart chambers once they are implanted, impairing cardiac filling and causing injury to the anatomy within the heart.

Thus, there remains a need for prosthetic heart valves that are smaller in size but that are still configured to assist or replace the functionality of a diseased or damaged native heart valve. In addition, there remains a need for prosthetic heart valves that are more easily maneuvered into the heart and securely implanted at the site of a native heart valve. Moreover, there remains a need for improved prosthetic heart valve delivery systems that are configured to securely implant a prosthetic heart valve at an implantation site. The present disclosure provides prosthetic heart valves with a reduced axial length such that the prosthetic heart valves may be more easily delivered into the heart and may exhibit less protrusion into the chambers of the heart. The present disclosure also provides improved prosthetic heart valve delivery systems and methods of implanting prosthetic heart valves, such that prosthetic heart valves may be securely anchored at the implantation site.

SUMMARY

The present disclosure discloses prosthetic valves for implantation within a native valve and methods for implanting prosthetic valves within a native valve. Particular examples of the disclosure may pertain to a prosthetic valve including ventricular tissue anchors and atrial tissue anchors having rigid portions. The ventricular tissue anchors and atrial tissue anchor rigid portions may be equal in length and exert opposing clamping forces on tissue to anchor the prosthetic valve within the native valve.

According to an exemplary embodiment of the present disclosure, a prosthetic valve configured for implantation within a native valve is provided. The prosthetic valve includes an expandable valve body having an inner lumen extending along a longitudinal axis of the valve body. The prosthetic valve additionally includes a plurality of ventricular tissue anchors configured to extend radially outward from the valve body to respective ventricular anchor distal ends. The prosthetic valve additionally includes a plurality of atrial tissue anchors configured to extend radially outward from the valve body to respective atrial anchor distal ends. Each atrial tissue anchor includes a rigid portion and a flexible portion situated between a distal end of the rigid portion and the atrial anchor distal end. The ventricular anchor distal end of at least one ventricular tissue anchor and the distal end of the rigid portion of at least one atrial tissue anchor are configured to be equidistant from the longitudinal axis of the valve body.

A portion of the at least one atrial tissue anchor is configured to be substantially aligned in a common lateral plane with a portion of the at least one ventricular tissue anchor. The distal end of the rigid portion of the at least one atrial tissue anchor is configured to be situated radially external to the portion of the at least one atrial tissue anchor aligned in the common lateral plane. Flexibility of the flexible portions of the atrial tissue anchors is imparted through a structure having multiple curves. The ventricular tissue anchors and the rigid portions of the atrial tissue anchors are devoid of the structure having multiple curves. The flexible portion of the at least one atrial tissue anchor includes a first segment configured to extend in a ventricular direction. The flexible portion of the at least one atrial tissue anchor additionally includes a second segment configured to extend in an atrial direction. The second segment of the flexible portion is configured to be situated radially external to the first segment of the flexible portion. An entire length of the at least one ventricular tissue anchor is configured to extend radially outward in an atrial direction. The ventricular anchor distal end of the at least one ventricular tissue anchor and the distal end of the rigid portion of the at least one atrial tissue anchor are configured to apply opposing grasping forces upon the native valve. The at least one ventricular tissue anchor includes a first opening. The first opening is situated within the widest portion of the at least one ventricular tissue anchor. The rigid portion of the at least one atrial tissue anchor includes a second opening. The second opening is situated within the widest portion of the rigid portion of the at least one atrial tissue anchor. The first opening and second opening are configured to be equidistant from the longitudinal axis of the valve body. The valve body includes an annular outer frame having an atrial end, a ventricular end opposite of the atrial end of the outer frame, and an intermediate portion extending between the atrial end of the outer frame and the ventricular end of the outer frame. The valve body additionally includes an inner frame situated at least partially within the outer frame, the inner frame having an atrial end, a ventricular end opposite of the atrial end of the inner frame, and an intermediate portion extending between the atrial end of the inner frame and the ventricular end of the inner frame. The ventricular tissue anchors extend from the intermediate portion of the outer frame and the atrial tissue anchors extend from the intermediate portion of the inner frame. The atrial tissue anchors are angularly offset from at least one location of connection between the outer frame and inner frame.

According to another exemplary embodiment of the present disclosure, a prosthetic valve configured for implantation within a native valve is provided. The prosthetic valve includes an expandable valve body. The prosthetic valve additionally includes a plurality of ventricular tissue anchors configured to extend radially outward from the valve body to respective ventricular anchor distal ends. The prosthetic valve additionally includes a plurality of atrial tissue anchors configured to extend radially outward from the valve body. Each atrial tissue anchor includes a rigid portion and a flexible portion. The flexible portion has a proximal end and a distal end configured to be situated radially external to the proximal end. The proximal end of the flexible portion is immediately adjacent to the rigid portion. The proximal end of the flexible portion of at least one atrial tissue anchor is configured to be situated radially external to the ventricular anchor distal ends of the plurality of ventricular tissue anchors.

A portion of the at least one atrial tissue anchor is configured to be substantially aligned in a common lateral plane with a portion of at least one ventricular tissue anchor. The proximal end of the flexible portion of the at least one atrial tissue anchor is configured to be situated radially external to the portion of the at least one atrial tissue anchor aligned in the common lateral plane. The rigid portion of the at least one atrial tissue anchor includes the portion of the at least one atrial tissue anchor aligned in the common lateral plane. Flexibility of the flexible portions of the atrial tissue anchors is imparted through a structure having multiple curves. The ventricular tissue anchors and the rigid portions of the atrial tissue anchors are devoid of the structure having multiple curves. The flexible portion of the at least one atrial tissue anchor includes a first segment configured to extend in a ventricular direction. The flexible portion of the at least one atrial tissue anchor additionally includes a second segment configured to extend in an atrial direction. The second segment of the flexible portion is configured to be situated radially external to the first segment of the flexible portion. An entire length of at least one ventricular tissue anchor is configured to extend radially outward in an atrial direction. The expandable valve body is configured to be implanted in the native valve independent of the rotational position of the atrial tissue anchors and ventricular tissue anchors relative to the native valve. The valve body includes an annular outer frame having an atrial end, a ventricular end opposite of the atrial end of the outer frame, and an intermediate portion extending between the atrial end of the outer frame and the ventricular end of the outer frame. The valve body additionally includes an inner frame situated at least partially within the outer frame. The inner frame includes an atrial end, a ventricular end opposite of the atrial end of the inner frame, and an intermediate portion extending between the atrial end of the inner frame and the ventricular end of the inner frame. The ventricular tissue anchors extend from the intermediate portion of the outer frame and the atrial tissue anchors extend from the intermediate portion of the inner frame. The atrial tissue anchors are angularly offset from at least one location of connection between the outer frame and inner frame.

Additional features and advantages of the disclosed embodiments will be set forth in part in the description that follows, and in part will be obvious from the description, or may be learned by practice of the disclosed embodiments. The features and advantages of the disclosed embodiments will be realized and attained by the elements and combinations particularly pointed out in the appended claims.

It is to be understood that both the foregoing general description and the following detailed description are examples and explanatory only and are not restrictive of the disclosed embodiments as claimed.

The accompanying drawings constitute a part of this specification. The drawings illustrate several embodiments of the present disclosure and, together with the description, serve to explain the principles of the disclosed embodiments as set forth in the accompanying claims.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1A illustrates a front elevation view of an exemplary frame for a prosthetic valve, consistent with various embodiments of the present disclosure.

FIG. 1B illustrates a perspective view of the exemplary frame of FIG. 1A, consistent with various embodiments of the present disclosure.

FIG. 2A illustrates a front elevation view of another exemplary frame for a prosthetic valve, consistent with various embodiments of the present disclosure.

FIG. 2B illustrates a top plan view of the exemplary frame of FIG. 2A, consistent with various embodiments of the present disclosure.

FIG. 2C illustrates an enlarged view of an atrial anchoring arm and a ventricular anchoring leg of the exemplary frame of FIG. 2A, consistent with various embodiments of the present disclosure.

FIG. 2D illustrates another front elevation view of the exemplary frame of FIG. 2A, consistent with various embodiments of the present disclosure.

FIG. 2E illustrates another top plan view of the exemplary frame of FIG. 2A, consistent with various embodiments of the present disclosure.

FIG. 3A illustrates a front elevation view of an inner frame of the exemplary frame of FIG. 2A, consistent with various embodiments of the present disclosure.

FIG. 3B illustrates an enlarged view of an atrial anchoring arm of the exemplary inner frame of FIG. 3A, consistent with various embodiments of the present disclosure.

FIG. 3C illustrates a front elevation view of an outer frame of the exemplary frame of FIG. 2A, consistent with various embodiments of the present disclosure.

FIG. 3D illustrates an enlarged view of a ventricular anchoring leg of the exemplary outer frame of FIG. 3C, consistent with various embodiments of the present disclosure.

FIG. 4A illustrates a cross-sectional view of the exemplary frame of FIG. 2A, consistent with various embodiments of the present disclosure.

FIG. 4B illustrates an enlarged view of a volume between an atrial anchoring arm and a ventricular anchoring leg of the exemplary frame of FIG. 4A, consistent with various embodiments of the present disclosure.

FIGS. 5A-5E illustrate structural changes in the exemplary frame of FIG. 2A during transitioning of the frame between a radially-contracted configuration and a radially-expanded configuration, consistent with various embodiments of the present disclosure.

FIG. 6A illustrates a front elevation view of an exemplary prosthetic valve, consistent with various embodiments of the present disclosure.

FIG. 6B illustrates a cross-sectional view of the exemplary prosthetic valve of FIG. 6A without leaflets, consistent with various embodiments of the present disclosure.

FIG. 6C illustrates a cross-sectional view of the exemplary prosthetic valve of FIG. 6A with leaflets, consistent with various embodiments of the present disclosure.

FIG. 6D illustrates a top plan view of the exemplary prosthetic valve of FIG. 6A with uninflated leaflets, consistent with various embodiments of the present disclosure.

FIG. 6E illustrates a top plan view of the exemplary prosthetic valve of FIG. 6A with inflated leaflets, consistent with various embodiments of the present disclosure.

FIG. 7A illustrates an exemplary prosthetic valve delivery system, consistent with various embodiments of the present disclosure.

FIG. 7B illustrates an enlarged view of a delivery capsule of the exemplary prosthetic valve delivery system of FIG. 7A, consistent with various embodiments of the present disclosure.

FIG. 7C illustrates an exemplary configuration of a telescoping catheter assembly and the delivery capsule of the exemplary prosthetic valve delivery system of FIG. 7A, consistent with various embodiments of the present disclosure.

FIG. 7D illustrates another exemplary configuration of the telescoping catheter assembly and delivery capsule of FIG. 7C, consistent with various embodiments of the present disclosure.

FIG. 8A illustrates another enlarged view of the exemplary delivery capsule of the prosthetic valve delivery system of FIG. 7A in a closed configuration, consistent with various embodiments of the present disclosure.

FIG. 8B illustrates the exemplary delivery capsule of FIG. 8A in an open configuration, consistent with various embodiments of the present disclosure.

FIG. 8C illustrates an interior view of the exemplary delivery capsule of FIG. 8A in the closed configuration, consistent with various embodiments of the present disclosure.

FIG. 9 illustrates advancement of the exemplary prosthetic valve delivery system of FIG. 7A into the left atrium, consistent with various embodiments of the present disclosure.

FIGS. 10A-10H depict implantation of the prosthetic valve of FIGS. 6A-6E within a native mitral valve by the exemplary prosthetic valve delivery system of FIG. 7A, consistent with various embodiments of the present disclosure.

DETAILED DESCRIPTION

Exemplary embodiments are described with reference to the accompanying drawings. In the figures, which are not necessarily drawn to scale, the left-most digit(s) of a reference number identifies the figure in which the reference number first appears. Wherever convenient, the same reference numbers are used throughout the drawings to refer to the same or like parts. While examples and features of disclosed principles are described herein, modifications, adaptations, and other implementations are possible without departing from the spirit and scope of the disclosed embodiments. Also, the words “comprising,” “having,” “containing,” and “including,” and other similar forms are intended to be equivalent in meaning and be open ended in that an item or items following any one of these words is not meant to be an exhaustive listing of such item or items, or meant to be limited to only the listed item or items. It should also be noted that as used in the present disclosure and in the appended claims, the singular forms “a,” “an,” and “the” include plural references unless the context clearly dictates otherwise.

In some embodiments of the present disclosure, an “atrial direction” may refer to a direction extending towards an atrium of the heart. For example, from a location within the left ventricle or the mitral valve, an atrial direction may refer to a direction extending towards the left atrium. Additionally, from a location within an atrium (e.g., the left atrium), an atrial direction may refer to a direction extending away from an adjacent atrioventricular valve (e.g., the mitral valve) and further into the atrium. For example, in FIGS. 10G and 10H, an atrial direction may refer to a direction extending upwards from prosthetic valve 6000 towards atrium 9010. In some exemplary embodiments, an atrial direction need not necessarily be parallel to a longitudinal axis of a prosthetic valve (e.g., longitudinal axis 2800 illustrated in FIG. 2A), so long as the direction is angled towards an atrium. The atrial direction may be parallel to a longitudinal axis of a prosthetic valve in some cases. In some embodiments, a “non-ventricular direction” may refer to a direction that does not extend towards a ventricle of the heart. A “non-ventricular direction” may extend in an atrial direction, or it may extend laterally in a direction perpendicular to a ventricular direction.

In some exemplary embodiments of the present disclosure, a “ventricular direction” may refer to a direction extending towards a ventricle of the heart. From a location within the left atrium or the mitral valve, a ventricular direction may refer to a direction extending towards the left ventricle. Additionally, from a location within a ventricle (e.g., the left ventricle), a ventricular direction may refer to a direction extending away from an adjacent atrioventricular valve (e.g., the mitral valve) and further into the ventricle. For example, in FIGS. 10G and 10H, a ventricular direction may refer to a direction extending downwards from prosthetic valve 6000 towards ventricle 9020. In some exemplary embodiments, a ventricular direction need not necessarily be parallel to a longitudinal axis of a prosthetic valve (e.g., longitudinal axis 2800 illustrated in FIG. 2A), so long as the direction is angled towards a ventricle. The ventricular direction may be parallel to a longitudinal axis of a prosthetic valve in some cases. In some embodiments, a “non-atrial direction” may refer to a direction that does not extend towards an atrium of the heart. A non-atrial direction may extend in a ventricular direction, or it may extend laterally in a direction perpendicular to an atrial direction.

Exemplary embodiments generally relate to prosthetic valves for implantation within a native valve and methods for implanting prosthetic valves within a native valve. In addition, exemplary embodiments generally relate to systems and methods for implantation of prosthetic valves by prosthetic valve delivery systems. While the present disclosure provides examples relating to prosthetic heart valves, and in particular prosthetic mitral valves, as well as delivery systems for prosthetic heart valves, it should be noted that aspects of the disclosure in their broadest sense are not limited to a prosthetic heart valve. Rather, the foregoing principles may be applied to other prosthetic valves as well. In various embodiments in accordance with the present disclosure, the term prosthetic valve refers generally to an implantable valve configured to restore and/or replace the functionality of a native valve, such as a diseased or otherwise impaired native heart valve.

An exemplary prosthetic valve may include a prosthetic valve configured to render a native valve structure non-functional, and may thus replace the function of the native valve. For example, an exemplary prosthetic valve may have a size and shape similar to the valve being replaced and may include a number of leaflet-like structures to regulate fluid flow and prevent backflow of blood through the valve. Additionally, or alternatively, an exemplary prosthetic valve may also include a prosthetic valve configured to leave the native valve structure intact and functional. An exemplary prosthetic valve may include a mitral valve, tricuspid valve, aortic valve, or pulmonary valve, as well as a valve outside of the heart, such as a venous valve, lymph node valve, ileocecal valve, or any other structure configured to control and/or regulate fluid flow in the body. An exemplary prosthetic valve may additionally or alternatively be configured to replace a failed bioprosthesis, such as a failed heart valve prosthesis.

FIG. 1A illustrates a front elevation view of an exemplary frame 1000 for a prosthetic valve. FIG. 1B illustrates a perspective view of frame 1000. Frame 1000 may be constructed of a shape memory material such as nickel titanium alloy (Nitinol) and may be configured to support other components of the prosthetic valve, such as prosthetic leaflets and protective cover layers. Frame 1000 may include an annular outer frame 1200 and an inner frame 1400 situated at least partially within the outer frame 1200. Annular outer frame 1200 and inner frame 1400 may be secured together by pins, screws, welding, soldering, adhesive, magnets, and/or any other suitable mechanism. For example, FIGS. 1A and 1B depict annular outer frame 1200 and inner frame 1400 connected by a plurality of connector pins 1040.

Annular outer frame 1200 may include an outer frame tubular portion 1220, which may be formed of a plurality of struts intersecting at junctions to form a wire mesh, stent-like, or cage-like structure of the outer frame tubular portion 1220. Annular outer frame 1200 may also include at least one ventricular anchoring leg 1240, which may be configured to extend radially outward from the outer frame tubular portion and which may contact, or otherwise engage, tissue within or near the native valve to anchor the prosthetic valve within the native valve. In some embodiments, exemplary valve frame 1000 may include twelve ventricular anchoring legs 1240, which may be configured to engage ventricular tissue of a native atrioventricular valve.

Inner frame 1400 may include an inner frame tubular portion 1420, which may be formed of a plurality of struts intersecting at junctions to form a wire mesh, stent-like, or cage-like structure of the inner frame tubular portion 1420. Inner frame 1400 may also include at least one atrial anchoring arm 1440, which may be configured to extend radially outward from the inner frame tubular portion and which may contact, or otherwise engage, tissue within or near the native valve to anchor the prosthetic valve within the native valve. In some embodiments, exemplary valve frame 1000 may include twelve atrial anchoring arms 1440, which may be configured to engage atrial tissue of a native atrioventricular valve.

Outer frame tubular portion 1220 and inner frame tubular portion 1420 may together form an annular valve body 1020 of the prosthetic valve, which may have at least one opening and from which the ventricular anchoring legs 1240 and atrial anchoring arms 1440 may extend. Annular valve body 1020 may include an axial lumen 1022 extending through the annular valve body 1020 along a longitudinal axis 1800 of the prosthetic valve. In some embodiments, annular valve body 1020 may be configured to receive a flow control device, such as one or more prosthetic leaflets, within axial lumen 1022. Optionally, annular valve body 1020 may include one or more atrial end delivery posts 1027 along an atrial end (i.e., top end) of the annular valve body and/or one or more ventricular end delivery posts 1028 along a ventricular end (i.e., bottom end) of the annular valve body. Delivery posts 1027 and 1028 may be configured to removably engage a delivery device of the prosthetic valve, for example, to assist with placement of frame 1000 within or near a native valve.

FIG. 2A illustrates a front view of another exemplary frame 2000 for a prosthetic valve. FIG. 2B illustrates a top plan view of the frame 2000. Frame 2000 may include an annular outer frame 2200 and an inner frame 2400 situated at least partially within the annular outer frame 2200. Annular outer frame 2200 and inner frame 2400 may be secured together by pins, screws, welding, soldering, adhesive, magnets, and/or any other suitable mechanism. For example, FIGS. 2A and 2B depict annular outer frame 2200 and inner frame 2400 connected by a plurality of connector pins 2040.

Annular outer frame 2200 may include an outer frame tubular portion 3605, which may be formed of a plurality of struts intersecting at junctions to form a wire mesh, stent-like, or cage-like structure of the outer frame tubular portion 3605. For example, as illustrated in FIG. 2A, annular outer frame 2200 may include outer frame atrial circumferential struts 3608 a, outer frame leg base struts 3608 b, and outer frame ventricular circumferential struts 3608 c intersecting at atrial end outer frame junctions 3602, leg attachment junctions 3802, outer frame junctions 3804, and ventricular end outer frame junctions 3604 to form outer frame tubular portion 3605. Annular outer frame 2200 may also include at least one ventricular anchoring leg 2240, which may extend from leg attachment junction 3802 of the outer frame tubular portion 3605 and which may be configured to engage ventricular tissue of a native valve to anchor the prosthetic valve in the native valve. The at least one ventricular anchoring leg 2240 may include a proximal leg end 3622, which may be the end of the leg connected to the outer frame tubular portion, and a distal leg end 2244, which may be situated radially outward from the outer frame tubular portion. As shown in FIG. 2B, the at least one ventricular anchoring leg 2240 may include at least one opening 2242.

Inner frame 2400 may include an inner frame tubular portion 3005, which may be formed of a plurality of struts intersecting at junctions to form a wire mesh, stent-like, or cage-like structure of the inner frame tubular portion 3005. For example, as illustrated in FIG. 2A, inner frame 2400 may include inner frame atrial struts 3008 a, inner frame intermediate struts 3008 b, and inner frame ventricular struts 3008 c intersecting at atrial end inner frame junctions 3002, arm attachment junctions 3202, inner frame strut junctions 3204, and ventricular end inner frame junctions 3004 to form inner frame tubular portion 3005. Inner frame 2400 may also include at least one atrial anchoring arm 2440, which may extend from arm attachment junction 3202 of the inner frame tubular portion 3005 and which may be configured to engage atrial tissue of a native valve to anchor the prosthetic valve in the native valve. The at least one atrial anchoring arm 2440 may include a proximal arm end 3020, which may be the end of the arm connected to the inner frame tubular portion, and a distal arm end 2444, which may be situated radially outward from the inner frame tubular portion. As shown in FIG. 2B, the at least one atrial anchoring arm 2440 may include a proximal arm opening 2441 and a distal arm opening 2442.

Outer frame tubular portion 3605 and inner frame tubular portion 3005 may together form an annular valve body 2020 of the prosthetic valve, which may have at least one opening and from which the ventricular anchoring legs 2240 and atrial anchoring arms 2440 may extend. Annular valve body 2020 may include an axial lumen 2022 extending through the annular valve body 2020 along a longitudinal axis 2800 of the prosthetic valve. Annular valve body 2020 may have an atrial end 2024, a ventricular end 2025 opposite the atrial end, and an intermediate portion 2026 extending between the atrial and ventricular ends. In some embodiments, the atrial end may refer to the portion of the annular valve body configured to be situated at a location within the atrium that is furthest from an adjacent ventricle, when the prosthetic valve is implanted in a native valve. Similarly, the ventricular end may refer to the portion of the annular valve body configured to be situated at a location within the ventricle that is furthest from an adjacent atrim, when the prosthetic valve is implanted in a native valve. The intermediate portion 2026 may extend between the atrial end 2024 and ventricular end 2025. In some embodiments, annular valve body 2020 may include one or more ventricular end delivery posts 1028 along the ventricular end 2025 of the annular valve body. Axial lumen 2022 may include an inlet opening 2032 at the atrial end of the annular valve body, as well as an outlet opening 2036 at the ventricular end of the annular valve body.

FIG. 2C illustrates an enlarged view of an atrial anchoring arm 2440 and a ventricular anchoring leg 2240 of frame 2000. Ventricular anchoring leg 2240 may include an inner, atrially-facing leg surface 2248 and an outer, ventricularly-facing leg surface 2249. Atrial anchoring arm 2440 may include an atrially-facing arm surface 2448 and a ventricularly-facing arm surface 2449. In some embodiments, atrial anchoring arm 2440 may include an arm portion 2446 configured to be arranged in a common lateral plane with leg portion 2246 of the ventricular anchoring leg 2240. That is, leg portion 2246 and arm portion 2446 may be positioned at the same axial position along longitudinal axis 2800.

FIG. 2D illustrates another front elevation view of frame 2000. The exemplary prosthetic valve, as well as frame 2000, may have an axial height 2560, which may extend between terminal arm ends 2444 and ventricular end 2025 of the annular valve body. Inner frame tubular portion 3005 may have an axial height 2530, which may extend between atrial end inner frame junctions 3002 and ventricular end inner frame junctions 3004. Annular outer frame 2200 may have an axial height 2550, which may extend between terminal leg ends 2244 and ventricular end 2025 of the annular valve body. Outer frame tubular portion 3605 may have an axial height 2570, which may extend between atrial end outer frame junctions 3602 and ventricular end outer frame junctions 3604. In some embodiments, frame 2000 may have a ventricular device protrusion distance 2540, which may represent the distance over which the prosthetic valve protrudes into a left ventricle when the prosthetic valve is implanted in a native mitral valve. Annular valve body 2020 may include a valve inlet radius 2520, which may be the radius of atrial inlet opening 2032.

FIG. 2E illustrates another top plan view of frame 2000. The atrial anchoring arms 2440 may have a length 2580, and the ventricular anchoring legs 2240 may have a length 2590. The terminal arm ends 2444 may define an atrial anchoring arm circumference 2640. The terminal leg ends 2244 may define a ventricular anchoring leg circumference 2620, which may be concentric with atrial anchoring arm circumference 2640. Inflexible portions 3402 of the atrial anchoring arms (illustrated in FIG. 3B) may have a length 2581. Serpentine structures 3406 of the atrial anchoring arms (illustrated in FIG. 3B) may have a length 2582.

FIG. 3A illustrates a front elevation view of inner frame 2400. The atrial end inner frame junctions 3002 and ventricular end inner frame junctions 3004 may form the atrial end and ventricular end, respectively, of inner frame 2400. Inner frame intermediate portion 3006 may extend between atrial end inner frame junctions 3002 and ventricular end inner frame junctions 3004. Inner frame tubular portion 3005 may have a radially inner surface 3018 and a radially outer surface 3016. Inner frame atrial struts 3008 a and inner frame intermediate struts 3008 b may intersect at atrial end inner frame junctions 3002, arm attachment junctions 3202, and strut junctions 3204 to form a first, atrial row of closed cells 3012. Inner frame intermediate struts 3008 b and inner frame ventricular struts 3008 c may intersect at arm attachment junctions 3202, strut junctions 3204, and ventricular end inner frame junctions 3004 to form a second, ventricular row of closed cells 3014. At least one inner frame atrial strut 3008 a may have a cross-sectional area 3010. At least one atrial anchoring arm 2440 may have a cross-sectional area 3022.

FIG. 3B illustrates an enlarged view of an atrial anchoring arm 2440 of inner frame 2400. Atrial anchoring arm 2440 may include a proximal arm portion 3502 configured to extend in an atrial direction, intermediate arm portion 3504 configured to extend in a ventricular direction, and distal arm portion 3506 configured to extend in an atrial direction. Arm transition portion 3508 may represent the transition between intermediate arm portion 3504 and distal arm portion 3506. Atrial anchoring arm 2440 may also include an inflexible portion 3402 extending to proximal arm end 3020, as well as a serpentine structure 3406, which may be situated radially external to the inflexible portion 3402. Inflexible portion 3402 may have a proximal end 3402 p, a distal end 3402 d, and a cross-sectional area 3402 c. Serpentine structure 3406 may have a cross-sectional area 3406 c. In some embodiments, atrial anchoring arm 2440 may include a terminal arm region 3408 situated radially external to serpentine structure 3406. Distal arm opening 2442 may be situated within terminal arm region 3408.

FIG. 3C illustrates a front elevation view of outer frame 2200. The atrial end outer frame junctions 3602 and ventricular end outer frame junctions 3604 may form the atrial end and ventricular end, respectively, of annular outer frame 2200. Outer frame intermediate portion 3606 may extend between atrial end outer frame junctions 3602 and ventricular end outer frame junctions 3604. Outer frame tubular portion 3605 may have a radially outer surface 3618 and a radially inner surface 3620. The outer frame atrial circumferential struts 3608 a, outer frame leg base struts 3608 b, and outer frame ventricular circumferential struts 3608 c may intersect at the atrial end outer frame junctions 3602, leg attachment junctions 3802, outer frame junctions 3804, and ventricular end outer frame junctions 3604 to form closed cells 3616. At least one outer frame atrial circumferential strut 3608 a may have a cross-sectional area 3610 and a width 3612. At least one outer frame leg base strut 3608 b may have a cross-sectional area 3614. At least one ventricular anchoring leg may have a cross-sectional area 3624 and a radially outer surface width 3626.

FIG. 3D illustrates an enlarged view of a portion of a ventricular anchoring leg 2240 of annular outer frame 2200. Ventricular anchoring leg 2240 may include a first, proximal curved portion 3807 and a second, distal curved portion 3808. In some embodiments, proximal curved portion 3807 may face radially outward. Additionally, or alternatively, distal curved portion 3808 may face radially inwards.

FIG. 4A illustrates a cross-sectional view of frame 2000, and FIG. 4B illustrates an enlarged view of a portion of FIG. 4A depicting a volume 4000 formed between the atrial anchoring arms 2440 and ventricular anchoring legs 2240. FIG. 4B also depicts an outer surface 4010 and inner surface 4020 of annular valve body 2020. In some embodiments, volume 4000 may be bounded by the ventricularly-facing surfaces 2449 of atrial anchoring arms 2440, by the inner, atrially-facing surfaces 2248 of ventricular anchoring legs 2240, and by the outer surface 4010 of the annular valve body 2020.

FIG. 5A illustrates a configuration of the exemplary prosthetic valve in which annular valve body 2020, atrial anchoring arms 2440, and ventricular anchoring legs 2240 are arranged in a radially-contracted configuration. In some embodiments, the configuration illustrated in FIG. 5A may constitute a radially-contracted configuration of the prosthetic valve.

FIG. 5B illustrates a configuration of the exemplary prosthetic valve in which annular valve body 2020 and atrial anchoring arms 2440 are arranged in a radially-contracted configuration. In the configuration of FIG. 5B, the ventricular anchoring legs 2240 may deflect radially outward away from annular valve body 2020, into a radially-expanded configuration of the ventricular anchoring legs 2240.

FIG. 5C illustrates a configuration of the exemplary prosthetic valve in which annular valve body 2020 and ventricular anchoring legs 2240 are arranged in a radially-contracted configuration. In the configuration of FIG. 5C, the atrial anchoring arms 2440 may deflect radially outward away from annular valve body 2020, into a radially-expanded configuration of the atrial anchoring arms 2440.

FIG. 5D illustrates a configuration of the exemplary prosthetic valve in which the atrial anchoring arms 2440 and ventricular anchoring legs 2240 may deflect radially outward away from annular valve body 2020 into their respective radially-expanded configurations, while annular valve body 2020 remains in a radially-contracted configuration. In the configuration of FIG. 5D, an axial distance 5004 may be formed between the atrial anchoring arms 2440 and the terminal ends 2244 of the ventricular anchoring legs 2240.

FIG. 5E illustrates a configuration of the exemplary prosthetic valve in which annular valve body 2020, atrial anchoring arms 2440, and ventricular anchoring legs 2240 are arranged in a radially-expanded configuration. In some embodiments, the configuration illustrated in FIG. 5E may constitute a radially-expanded configuration of the prosthetic valve.

FIG. 6A illustrates a front elevation view of prosthetic valve 6000. In some embodiments, prosthetic valve 6000 may be assembled upon frame 2000. Prosthetic valve 6000 may be configured for implantation within or near a native valve structure and may be configured to restore and/or replace the functionality of a native valve, such as a diseased or otherwise impaired native valve. Prosthetic valve 6000 may include valve frame 2000, including annular valve body 2020, the atrial anchoring arms 2440, and the ventricular anchoring legs 2240. Prosthetic valve 6000 may also include a skirt layer 6100 configured around an external surface of a portion of the annular valve body. Prosthetic valve 6000 may additionally include a first cuff sheet 6210, which may be connected to skirt layer 6100 via stitching 6104, as well as a second cuff sheet 6220, which may be connected to first cuff sheet 6210 via stitching 6420. In some embodiments, the first cuff sheet 6210 and second cuff sheet 6220 by extend around the terminal ends 2444 of the atrial anchoring arms 2440. Skirt layer 6100, first cuff sheet 6210, and second cuff sheet 6220 may be constructed of fluid-impermeable material and may accordingly be configured to prevent passage of blood or other fluids through portions of the prosthetic valve 6000 outside of the axial lumen 2022.

In some embodiments, prosthetic valve 6000 may additionally include a protective sleeve 6102 wrapped around the rim 6800 of the ventricular outlet opening of annular valve body 2020; protective sleeve 6102 may be secured to annular valve body 2020 by stitching 6108. Additionally, or alternatively, prosthetic valve 6000 may include at least one liner 6310 extending around an external surface of the ventricular anchoring legs 2240, with at least one protective layer 6330 positioned around the distal leg ends 2244 and at least one protective covering 6320 wrapped around the proximal leg ends 3622. In some embodiments, the at least one protective covering 6320 may be secured to the skirt layer 6100 via stitching 6322.

FIG. 6B illustrates a cross-sectional view of prosthetic valve 6000, without prosthetic leaflets situated within the axial lumen 2022. As illustrated in FIG. 6B, prosthetic valve 6000 may additionally include a liner 6400 covering at least a portion of the inner surface 4020 of the annular valve body 2020. Liner 6400 may be secured to the annular valve body 2020 via stitching 6430 and to the second cuff sheet 6220 via stitching 6410. First cuff sheet 6210, second cuff sheet 6220, and inner liner 6400 may together form an inflatable cuff 6200 having an interior volume 6500. In some embodiments, inflatable cuff 6200 may be secured to atrial anchoring arm 2440 via connector 6440. Blood may enter the cuff 6200 through openings 6230, causing the cuff 6200 to inflate radially outwards and axially in an atrial direction. In some embodiments, cuff 6200 may inflate radially outwards and press against tissue of the native valve. This engagement between the cuff and tissue of the native valve may form a barrier to flow of blood and other fluids around the outer circumference of the prosthetic valve 6000.

FIG. 6C illustrates a cross-sectional view of prosthetic valve 6000 with prosthetic leaflets 6602 and 6604 situated within the axial lumen 2022. In some embodiments, prosthetic valve 6000 may also include a third prosthetic leaflet 6606, which may not be visible in the view of FIG. 6C. The leaflets 6602, 6604, and 6606 may be secured to inner liner 6400 via stitching 6608 and may include a connector 6610 wrapping around the ventricular end delivery posts 2028 to secure the leaflets 6602, 6604, and 6606 to the valve frame 2000.

FIG. 6D illustrates a top plan view of prosthetic valve 6000, with leaflets 6602, 6604, and 6606 arranged in an open, uninflated configuration. In the open configuration, a space may be formed in the middle of the leaflets, permitting fluid to pass through the axial lumen 2022 of the prosthetic valve 6000. FIG. 6E illustrates a top plan view of prosthetic valve 6000, with leaflets 6602, 6604, and 6606 arranged in a closed, coapted configuration. In the closed configuration, the leaflets may press together such that the opening between them is closed. For example, the point of contact 6007 between two adjacent leaflets may extend to the center of the axial lumen; as a result, the leaflets may block fluid passage through the axial lumen 2022 of the prosthetic valve 6000.

FIG. 7A illustrates a prosthetic valve delivery system 7000. Delivery system 7000 may be configured to deliver an implant prosthetic valve 6000 within a native valve, such as a native mitral valve. Prosthetic valve delivery system 7000 may include a control handle assembly 7100, a telescoping catheter assembly 7200, a delivery capsule 7300 configured to retain a prosthetic valve (e.g. valve 6000), and, optionally, a stand 7400.

Control handle assembly 7100 may include an outer sheath control handle 7120 having a steering knob 7122 configured to steer an outer sheath 7210 of the telescoping catheter assembly 7200. Control handle assembly 7100 may also include a guide catheter control handle 7140 having a steering knob 7142 configured to steer a guide catheter 7220 of the telescoping catheter assembly 7200.

Control handle assembly 7100 may also include an implant catheter control handle 7160 having a steering knob 7168 configured to steer an implant catheter 8100 of the telescoping catheter assembly 7200. Implant catheter control handle 7160 may also include a proximal capsule portion slider 7162, a distal capsule portion knob 7170, and a distal capsule portion knob lock 7172 configured to control release of the prosthetic valve 6000 from within delivery capsule 7300. Implant catheter control handle 7160 may also include a slide lock 7166 configured to lock the implant catheter control handle 7160 at a position within track 7420 of stand 7400.

Control handle assembly 7100 may also include a cradle 7180, which may be secured to stand 7400 via a locking mechanism that can be released by actuated of release button 7184. Cradle 7180 may include a rotation knob 7182 configured to control rotation of the outer sheath 7210 and guide catheter 7220. Cradle 7180 may also include a rotation knob 7186 configured to control rotation of the implant catheter 8100. Cradle 7180 may also include a knob 7188 configured to control relative axial movement between outer sheath control handle 7120 (which may be secured to outer sheath 7210) and guide catheter control handle 7140 (which may be secured to guide catheter 7220).

FIG. 7B illustrates an enlarged view of delivery capsule 7300 of prosthetic valve delivery system 7000. Delivery capsule 7300 may include a proximal capsule portion 7320 and a distal capsule portion 7340 with a nose cone 7360 secured to the distal capsule portion 7340. A nose cone distal tip 7365 may form the distal end of the delivery capsule 7300. The telescoping catheter assembly 7200 may include a capsule shaft 7230 secured to, and configured to control movement of, the proximal capsule portion 7320 (e.g., due to connection 8400 between the capsule shaft 7230 and proximal capsule portion 7320, as illustrated in FIG. 8C). Implant catheter 8100 may extend within proximal capsule portion 7320 and may have a valve anchor disc 8200 connected to the distal end of the implant catheter 8100. A torque shaft 8300 may extend from the implant catheter 8100 and may be connected to distal capsule portion 7340; accordingly, torque shaft 8300 may be configured to control axial movement of the distal capsule portion 7340 relative to the implant catheter 8100 and valve anchor disc 8200. The proximal capsule portion 7320 and a distal capsule portion 7340 may be configured to retain prosthetic valve 6000, with the prosthetic valve 6000 secured against axial movement by valve anchor disc 8200. Control handle assembly 7100 may be configured to control movement of the proximal capsule portion 7320 and a distal capsule portion 7340, and thus may also control release of the prosthetic valve 6000 from within the delivery capsule 7300.

FIGS. 7C and 7D illustrate exemplary configurations of the telescoping catheter assembly 7200. Outer sheath 7210 and guide catheter 7220 may include respective bending portions 7215 and 7225, at which the outer sheath 7210 and guide catheter 7220 may be configured to bend within their respective steering planes 7212 and 7222. In some embodiments, bending of the outer sheath 7210 within the first steering plane 7212 may be controlled by the outer sheath steering knob 7122 of the control handle assembly 7100. Additionally, or alternatively, bending of the guide catheter 7220 within the second steering plane 7222 may be controlled by the guide catheter steering knob 7142 of the control handle assembly 7100. In some embodiments, under control of the control handle assembly 7100, the outer sheath 7210, guide catheter 7220, and implant catheter 8100 may be steered so as to correctly position the delivery capsule 7300 within a native valve for implantation of the prosthetic valve.

FIG. 8A illustrates an enlarged view of delivery capsule 7300 in a closed configuration, while FIG. 8B illustrates an enlarged view of delivery capsule 7300 in an open configuration. In the closed configuration of FIG. 8A, the distal capsule portion 7340 and proximal capsule portion 7320 may be brought together to form an enclosed compartment in which prosthetic valve 6000 may be retained. In the open configuration of FIG. 8B, the distal capsule portion 7340 and proximal capsule portion 7320 may be drawn apart. In some embodiments, the delivery capsule 7300 may be configured such that the distal capsule portion 7340 and proximal capsule portion 7320 are moved apart from each other, the prosthetic valve 6000 may be sequentially deployed from within the delivery capsule and implanted within a native valve.

FIG. 8C illustrates an interior view of delivery capsule 7300 with prosthetic valve 6000 retained within the delivery capsule. Although only the valve frame 2000 of the prosthetic valve 6000 is illustrated in FIG. 8C, one of ordinary skill will understand that the entire prosthetic valve 6000 depicted in FIGS. 6A-6E may be retained within delivery capsule 7300 in the configuration illustrated in FIG. 8C.

In the embodiment illustrated in FIG. 8C, at least a portion of the annular valve body 2020 and ventricular anchoring legs 2240 of the prosthetic valve 6000 may be retained within the distal capsule portion. Additionally, or alternatively, at least a portion of atrial anchoring arms 2440 may be retained within proximal capsule portion 7320. In some embodiments, valve anchor disc 8200 may include a number of recesses 8205 configured to receive and retain the ventricular end delivery posts 2028 of the prosthetic valve 6000. For example, the valve anchor disc 8200 may include at least the same number of recesses 8205 as there are delivery posts 2028 of the prosthetic valve 6000. In some embodiments, the delivery posts 2028 may be retained within the recesses 8205 so long as the annular valve body 2020 remains in a radially-contracted configuration; the engagement between the valve anchor disc 8200 and delivery posts 2028 may secure the prosthetic valve 6000 against axial movement. Upon radial expansion of the annular valve body 2020, the delivery posts 2028 may slide or expand out of the recesses 8205, freeing the prosthetic valve 6000 from engagement with the valve anchor disc 8200.

FIG. 9 illustrates one exemplary advancement route of the delivery capsule 7300 to the left atrium. In the example illustrated in FIG. 9, the delivery capsule 7300 may be steered through the vena cava into the right atrium 9210 and may pierce the interatrial septum and enter the left atrium 9010. Alternatively, the delivery capsule may be delivered to the heart by other routes. FIG. 9 also depicts the left ventricle 9020, the mitral valve 9030, the chordae tendineae 9022, the aortic valve 9045, and the aorta 9040.

FIGS. 10A-10H depict an exemplary implantation method of prosthetic valve 6000 within a mitral valve 9030. In FIG. 10A, the delivery capsule 7300 may be coaxially aligned with the mitral valve 9030. In some embodiments, the prosthetic valve 6000 may be held within the delivery capsule 7300 while the prosthetic valve is arranged in the configuration of FIG. 5A. In FIG. 10B, the delivery capsule 7300 may be distally advanced into the mitral valve 9030. In FIG. 10C, the distal capsule portion 7340 may be distally advanced relative to the rest of the delivery capsule 7300. This may release the ventricular anchoring legs 2240 from the distal capsule portion 7340, while the atrial anchoring arms 2440 and annular valve body 2020 remain constrained within the delivery capsule. In the example shown in FIG. 10C, the ventricular anchoring legs 2240 may be released from the delivery capsule 7300 within the atrium 9010. In some embodiments, the prosthetic valve 6000 may assume the configuration of FIG. 5B when the ventricular anchoring legs 2240 are released in the step depicted in FIG. 10C.

In FIG. 10D, the released ventricular anchoring legs 2240 may be passed through the mitral valve 9030 and into the left ventricle 9020. In FIG. 10E, the released legs 2240 may be proximally retracted until the ventricular anchoring legs come into contact with the ventricular tissue of the mitral valve 9030. In FIG. 10F, the proximal capsule portion 7320 may be retracted proximally, thus releasing the atrial anchoring arms 2440 within atrium 9010 while the annular valve body 2020 remains radially constrained within the distal capsule portion 7340. In some embodiments, the prosthetic valve 6000 may assume the configuration of FIG. 5D when the atrial anchoring arms 2440 are released in the step of FIG. 10F.

In FIG. 10G, the distal capsule portion 7340 may be advanced further until the annular valve body 2020 is released from the capsule and allowed to radially expand. Radial expansion of the annular valve body 2020 may allow the prosthetic valve to assume the fully-expanded configuration illustrated in FIG. 5E. At this stage, prosthetic valve 6000 may be securely implanted within mitral valve 9030. In FIG. 10H, the delivery system 7000, including capsule 7300, may be removed.

Various embodiments of the present disclosure relate to prosthetic valves, including prosthetic heart valves. While the present disclosure provides examples of prosthetic heart valves, and in particular prosthetic mitral valves, it should be noted that aspects of the disclosure in their broadest sense are not limited to a prosthetic heart valve. Rather, the foregoing principles may be applied to other prosthetic valves as well. Prosthetic heart valve 6000, illustrated in FIGS. 6A-6E, is one example of a prosthetic valve in accordance with the present disclosure.

In some embodiments, an exemplary prosthetic valve may be configured for implantation within a native valve, such as a mitral valve, tricuspid valve, aortic valve, or pulmonary valve. For example, the exemplary prosthetic valve may be configured for implantation within a native atrioventricular valve and may be configured to regulate blood flow between the atrium and ventricle. For example, prosthetic heart valve 6000 illustrated in FIGS. 6A-6C may include a fluid-impervious cuff 6200 configured to extend from an inner lumen 2022 of the prosthetic valve to terminal arm ends 2444 of a plurality of atrial anchoring arms 2440. Because cuff 6200 is constructed of a fluid-impervious material, cuff 6200 may be configured to minimize or block flow of blood and other fluids through any portion of the prosthetic valve 6000 except for lumen 2022. In addition, atrial anchoring arms 2440 of the prosthetic valve (including terminal arm ends 2444) may be configured to contact and, in some embodiments, press against atrial tissue of a native heart valve. This is illustrated in FIGS. 10G-10H, which depict atrial anchoring arms 2440 of prosthetic valve 6000 arranged in contact with, and exerting a ventricularly-directed force (that is, a force directed downwards toward ventricle 9020) upon atrial tissue of native mitral valve 9030. As a result, cuff 6200 of prosthetic valve 6000 may also be configured to minimize or block passage of blood and other fluids between the prosthetic valve 6000 (including terminal arm ends 2444) and native valve tissue, a condition known as perivalvular leakage. As a result, prosthetic valve 6000 may be configured to prohibit passage of blood and other fluids between atrium 9010 and ventricle 9020, except by passage through inner lumen 2022, in which leaflets 6602, 6604, and 6606 may be situated.

In some embodiments, an exemplary prosthetic valve may be expandable, such as between a radially-contracted configuration (e.g., a crimped state) and a radially-expanded configuration. For example, FIG. 5A illustrates a radially-contracted configuration of an exemplary prosthetic valve, and FIG. 5E illustrates a radially-expanded configuration of the exemplary prosthetic valve. The diameter of the prosthetic valve, including annular valve body 2020, ventricular anchoring legs 2240, and atrial anchoring arms 2440, may be reduced when the prosthetic valve assumes the radially-contracted configuration, as illustrated in FIG. 5A. Conversely, the diameter of the prosthetic valve may be increased when the prosthetic valve assumes the radially-expanded configuration, as illustrated in FIG. 5E. For example, the annular valve body 2020 of the prosthetic valve may radially expand when the prosthetic valve assumes the radially-expanded configuration. Additionally, or alternatively, the ventricular anchoring legs 2240 and/or atrial anchoring arms 2440 may be configured to deflect radially outward from the annular valve body 2020 when the prosthetic valve assumes the radially-expanded configuration.

In some embodiments, the exemplary prosthetic valve may be configured to be radially contracted into a radially-contracted configuration for introduction to an implantation site, such as on or within a delivery device. Accordingly, in some embodiments, the radially-contracted configuration may also be a delivery configuration, in which the prosthetic valve is arranged for delivery to the implantation site. Once at or near the implantation site, the prosthetic valve may be radially expanded to a radially-expanded configuration, in which the prosthetic valve may be anchored at the implantation site. Accordingly, in some embodiments, the radially-expanded configuration may also be a deployed configuration, in which the prosthetic valve is released from the delivery tool and seated at the implantation site.

In some embodiments, an exemplary prosthetic valve may be configured for self-expansion to the radially-expanded configuration; that is, the prosthetic valve may be biased to assume the radially-expanded configuration due to, at least in part, the design and/or material composition of the prosthetic valve. The self-expanding prosthetic valve may be constructed of a shape memory material such as nickel titanium alloy (Nitinol), which may permit the prosthetic valve to expand to a pre-determined diameter upon removal of a constraining force and/or application of heat or energy. For example, the prosthetic valve may be contracted and held in the radially-contracted configuration by a constraining device, such as a sheath, catheter, stent, or delivery capsule. An example of such a constraining device is illustrated in FIG. 8C, which illustrates prosthetic heart valve 6000 held in a radially-contracted configuration within delivery capsule 7300. When the prosthetic valve is positioned at or near the implantation site, the constraining force may be removed and the prosthetic valve allowed to self-expand to the radially-expanded configuration. Additionally, or alternatively, an exemplary prosthetic valve may be configured to expand due to application of radially expansive forces thereupon. For example, the prosthetic valve may be placed, in its radially-contracted configuration, upon an expansion device such as a balloon catheter. Upon positioning at the implantation site, the expansion device may exert an outwardly-directed force upon the prosthetic valve, causing it to expand to the radially-expanded configuration.

In some embodiments, the exemplary prosthetic valve may be configured for implantation at a treatment site within the body, such as within or adjacent to a native valve. In some embodiments, a prosthetic valve may be configured for transcatheter delivery to the implantation site via a variety of approaches, such as transapically, transatrially, and/or transseptally. In some embodiments, the prosthetic valve may be configured for implantation in the annulus or orifice of a native valve structure (e.g., a native heart valve). For example, in FIGS. 10A-10H, prosthetic valve 6000 may be delivered to and expanded within native mitral valve 9030 such that prosthetic valve 6000 is anchored within native mitral valve 9030. In some embodiments, the exemplary prosthetic valve may be configured to grasp tissue of the native valve to more firmly anchor the prosthetic valve within the native valve. For example, an exemplary prosthetic valve may be configured to grasp native leaflets and/or the native valve annulus to firmly seat the prosthetic valve within the valve annulus, thus preventing the prosthetic valve from migrating or dislodging from within the native valve annulus.

In some embodiments, the exemplary prosthetic valve may include a valve body. The valve body may be configured to receive or otherwise support a flow control device, such as one or more leaflets, for regulating flow of blood or other bodily fluids through the prosthetic valve. For example, the flow control device (e.g., leaflets) may be secured directly to the valve body and/or to an intermediate structure that is in turn secured to the valve body. As a result, when the prosthetic valve is implanted within a native valve, the flow control device (e.g., leaflets) may regulate fluid passage through the native valve, thus restoring and/or replacing the functionality of the native valve. For example, FIGS. 6D and 6E illustrate an exemplary prosthetic heart valve 6000 including an annular valve body 2020 (i.e., the exemplary valve body) with prosthetic leaflets 6602, 6604, and 6606 received within the annular valve body. In the example of a prosthetic mitral valve, the flow control device of the valve body may be configured to permit flow of blood and other fluids in one direction (e.g., from the left atrium to the left ventricle) and to prevent flow of blood and other fluids in a second, opposite direction (e.g., from the left ventricle to the left atrium).

In some embodiments, the valve body may be annular or ring-shaped and may include an inner lumen extending through the valve body. In some embodiments, the inner lumen of the valve body may extend along a longitudinal axis of the valve body. For example, FIG. 2B illustrates an exemplary frame 2000 of a prosthetic heart valve. Heart valve frame 2000 may include an annular valve body 2020 (i.e., the exemplary valve body) having an axial lumen 2022 extending along the entire length of annular valve body 2020. In some embodiments, axial lumen 2022 may extend along longitudinal axis 2800 of valve body 2020, illustrated in FIG. 2A. The valve body may be sized and configured to be seated within the orifice of a native valve. For example, as depicted in FIG. 10H, annular valve body 2020 may be situated within the orifice of mitral valve 9030, specifically between native leaflets 9032. In some embodiments, the valve body may be configured to have a smaller diameter, when fully-expanded, than the diameter of the orifice of the native valve. In such embodiments, the valve body may be anchored in the native valve by anchoring structures, such as atrial anchoring arms and/or ventricular anchoring legs. Alternatively, the valve body may be configured to expand to an equal or greater diameter than the diameter of the native valve orifice such that the valve body is anchored within the native valve.

The valve body may have a circular, oval-shaped, elliptical, or D-shaped cross-section and may be symmetrical about at least one axis of the valve body. For example, FIG. 2B illustrates exemplary annular valve body 2020 (i.e., the exemplary valve body), which may have a substantially circular cross-section and which may be symmetrical about longitudinal axis 2800. Alternatively, the valve body may have any suitable cross-sectional shape with at least one opening within the valve body. In some embodiments, at least a portion of the valve body may be cylindrical, with a substantially constant diameter along the entire longitudinal length of the valve body. Alternatively, the valve body may have a variable diameter at different portions of the valve body (e.g., at different longitudinal portions of the valve body). For example, exemplary annular valve body 2020 illustrated in FIGS. 2A and 2D may have a diameter at a longitudinally central portion thereof (that is, in a middle portion of the annular valve body relative to longitudinal axis 2800) that may be larger than the diameter of the annular valve body 2020 at the atrial end 2024 of the annular valve body (i.e., the top of annular valve body 2020 in FIG. 2A) and/or the diameter of the annular valve body 2020 at the ventricular end 2025 of the annular valve body (i.e., the bottom of annular valve body 2020 in FIG. 2A). Advantageously, such a configuration may improve the seating of the valve body within the native valve orifice, providing an improved pressure fit therebetween.

In some embodiments, the valve body may be expandable, such as between a radially-contracted configuration and a radially-expanded configuration. For example, the valve body may be configured to radially expand independently of other components of the exemplary prosthetic valve. For example, the valve body may be configured to remain in a radially-contracted configuration while other components of the prosthetic valve, such as one or more tissue anchors, are deployed radially outward. For example, FIG. 5B depicts an exemplary annular valve body 2020 (i.e., the exemplary valve body) arranged in a radially-contracted configuration while a plurality of ventricular anchoring legs 2240, and in particular the distal leg ends 2244 of the ventricular anchoring legs 2240, are deployed radially outward (e.g., due to removal of a constraining delivery device from the ventricular anchoring legs). In the configuration illustrated in FIG. 5B, the heart valve frame 2000 may additionally include a plurality of atrial anchoring arms 2440 configured in a radially-contracted configuration. Similarly, FIG. 5C depicts an exemplary configuration in which the annular valve body 2020 and a plurality of ventricular anchoring legs 2240 may be arranged in a radially-contracted configuration, while a plurality of atrial anchoring arms 2440, and in particular the terminal arm ends 2444 of the atrial anchoring arms 2440, are deployed radially outward (e.g., due to removal of a constraining delivery device from the atrial anchoring arms). Further, FIG. 5D depicts an exemplary configuration in which the annular valve body 2020 may be arranged in a radially-contracted configuration, while the plurality of atrial anchoring arms 2440 and the plurality of ventricular anchoring legs 2240 are deployed radially outward.

In some embodiments, the exemplary prosthetic valve may include a plurality (that is, one or more) of ventricular tissue anchors configured to extend radially outward from the valve body. For example, FIG. 2A illustrates an annular valve body 2020 (i.e., the exemplary valve body) and a plurality of ventricular anchoring legs 2240 extending radially outward from the annular valve body. Accordingly, ventricular anchoring legs 2240 may constitute the ventricular tissue anchors, in some embodiments. The ventricular tissue anchors may be configured to anchor the prosthetic valve at an implantation site, such as within or near a native valve. For example, the ventricular tissue anchors may be configured to engage ventricular tissue of a native mitral valve to anchor the prosthetic valve within the mitral valve. In some embodiments, the ventricular tissue anchors may be configured to be positioned at least partially within a ventricle upon implantation of the prosthetic valve within or near a native mitral valve, and to engage ventricular tissue of the mitral valve. For example, FIGS. 10E-10H depict ventricular anchoring legs 2240 of an exemplary prosthetic heart valve 6000. Ventricular anchoring legs 2240 are situated within ventricle 9020 and may engage the ventricular side of native mitral valve 9030 to secure prosthetic heart valve 6000 within the mitral valve.

The prosthetic valve may include one ventricular tissue anchor, two ventricular tissue anchors, three ventricular tissue anchors, four ventricular tissue anchors, five ventricular tissue anchors, six ventricular tissue anchors, seven ventricular tissue anchors, eight ventricular tissue anchors, nine ventricular tissue anchors, ten ventricular tissue anchors, eleven ventricular tissue anchors, twelve ventricular tissue anchors, thirteen ventricular tissue anchors, fourteen ventricular tissue anchors, fifteen ventricular tissue anchors, sixteen ventricular tissue anchors, seventeen ventricular tissue anchors, eighteen ventricular tissue anchors, nineteen ventricular tissue anchors, twenty ventricular tissue anchors, or any other suitable number of ventricular tissue anchors. For example, exemplary prosthetic valve 6000 depicted in FIG. 2B includes twelve ventricular anchoring legs 2240 (i.e., the exemplary ventricular tissue anchors).

In some embodiments, the ventricular tissue anchors may be configured to extend radially outward from the valve body to respective ventricular anchor distal ends. In some embodiments, the term “radially outward” may refer to a direction extending away from the center of the valve body (for example, away from the longitudinal axis of the exemplary valve body). In some embodiments, the ventricular tissue anchors may be connected to the valve body and configured to extend radially outward from the valve body. For example, in FIGS. 5D and 5E, ventricular anchoring legs 2240 (i.e., the exemplary ventricular tissue anchors) may be connected to annular valve body 2020 (i.e., the exemplary valve body) at leg attachment junctions 3802 and may extend radially outward from the annular valve body 2020 to distal leg ends 2244 (i.e., exemplary ventricular anchor distal ends). In some embodiments, the ventricular tissue anchors may be physically connected to the valve body, such as by welding or adhesive. In some alternative embodiments, the ventricular tissue anchors may be integrally formed with the valve body. In some further alternative embodiments, the ventricular tissue anchors may not be secured directly to the valve body; however, the ventricular tissue anchors may be configured to extend in a radially outward direction from the valve body.

In some embodiments, the locations of connection between the ventricular tissue anchors and valve body may be spaced at a regular interval about a circumference of the valve body. For example, in FIG. 2A, the ventricular anchoring legs 2240 may extend from the annular valve body 2020 (i.e., the exemplary valve body) at leg attachment junctions 3802. Leg attachment junctions 3802 may be spaced at a regular interval about the circumference of annular valve body 2020. Additionally, or alternatively, the locations of connection between the ventricular tissue anchors and valve body may be arranged along a plane perpendicular to the longitudinal axis of the valve body. For example, in FIG. 2A, the leg attachment junctions 3802 may be arranged along a plane perpendicular to longitudinal axis 2800. That is, the leg attachment junctions 3802 may be situated at the same axial position along longitudinal axis 2800.

In some embodiments, each ventricular tissue anchor may include a ventricular anchor proximal end connected to or otherwise secured relative to the valve body, and a ventricular anchor distal end configured to extend radially outward from the valve body and, thus, from the ventricular anchor proximal end of the ventricular tissue anchor. In various embodiments, the term “proximal” refers to a portion of a feature (e.g., a ventricular tissue anchor) situated in closest proximity to the valve body and may, in some embodiments, include a point of connection between the feature (e.g., the ventricular tissue anchor) and the valve body. In various embodiments, the term “distal” refers to a portion of a feature (e.g., a ventricular tissue anchor) furthest from the point of connection between that feature and the valve body. For example, ventricular anchoring legs 2240 (i.e., the exemplary ventricular tissue anchors) illustrated in FIGS. 2A and 3C may include a proximal leg end 3622 connected to annular valve body 2020 (e.g., at leg attachment junction 3802) and a distal leg end 2244 (i.e., an exemplary ventricular anchor distal end) configured to extend radially outward from the annular valve body 2020 and from the proximal leg end 3622.

In some embodiments, the exemplary prosthetic valve may include a plurality (that is, one or more) of atrial tissue anchors configured to extend radially outward from the valve body. For example, FIG. 2A illustrates an annular valve body 2020 (i.e., the exemplary valve body) and a plurality of atrial anchoring arms 2440 extending radially outward from the valve body. The atrial tissue anchors may be configured to anchor the prosthetic valve at an implantation site, such as within or near a native valve. For example, the atrial tissue anchors may be configured to engage atrial tissue of a native mitral valve to anchor the prosthetic valve within the mitral valve. In some embodiments, the atrial tissue anchors may be configured to be positioned at least partially within an atrium upon implantation of the prosthetic valve within or near a native mitral valve, and to engage atrial tissue of the mitral valve. For example, FIGS. 10F-10H depict atrial anchoring arms 2440 of an exemplary prosthetic heart valve 6000. Atrial anchoring arms 2440 are situated within atrium 9010 and may engage the atrial side of native mitral valve 9030 to secure prosthetic heart valve 6000 within the mitral valve.

The prosthetic valve may include one atrial tissue anchor, two atrial tissue anchors, three atrial tissue anchors, four atrial tissue anchors, five atrial tissue anchors, six atrial tissue anchors, seven atrial tissue anchors, eight atrial tissue anchors, nine atrial tissue anchors, ten atrial tissue anchors, eleven atrial tissue anchors, twelve atrial tissue anchors, thirteen atrial tissue anchors, fourteen atrial tissue anchors, fifteen atrial tissue anchors, sixteen atrial tissue anchors, seventeen atrial tissue anchors, eighteen atrial tissue anchors, nineteen atrial tissue anchors, twenty atrial tissue anchors, or any other suitable number of atrial tissue anchors. For example, exemplary prosthetic valve 6000 depicted in FIG. 2B includes twelve atrial anchoring arms 2440 (i.e., the exemplary atrial tissue anchors).

In some embodiments, the atrial tissue anchors may be configured to extend radially outward from the valve body to respective atrial anchor distal ends. In some embodiments, the atrial tissue anchors may be connected to the valve body and configured to extend radially outward from the valve body. For example, in FIGS. 5D and 5E, atrial anchoring arms 2440 (i.e., the exemplary atrial tissue anchors) may be connected to annular valve body 2020 (i.e., the exemplary valve body) at arm attachment junctions 3202 and may extend radially outward from the annular valve body 2020. In some embodiments, the atrial tissue anchors may be physically connected to the valve body, such as by welding or adhesive. In some alternative embodiments, the atrial tissue anchors may be integrally formed with the valve body. In some further alternative embodiments, the atrial tissue anchors may not be secured directly to the valve body; however, the atrial tissue anchors may be configured to extend in a radially outward direction from the valve body.

In some embodiments, the locations of connection between the atrial tissue anchors and valve body may be spaced at a regular interval about a circumference of the valve body. For example, in FIG. 2A, the atrial anchoring arms 2440 (i.e., the exemplary atrial tissue anchors) may extend from the annular valve body 2020 at arm attachment junctions 3202. Arm attachment junctions 3202 may be spaced at a regular interval about the circumference of annular valve body 2020. Additionally, or alternatively, the locations of connection between the atrial tissue anchors and valve body may be arranged along a plane perpendicular to the longitudinal axis of the valve body. For example, in FIG. 2A, the arm attachment junctions 3202 may be arranged along a plane perpendicular to longitudinal axis 2800. That is, the arm attachment junctions 3202 may be situated at the same axial position along longitudinal axis 2800.

In some embodiments, each atrial tissue anchor may include an atrial anchor proximal end connected to or otherwise secured relative to the valve body, and an atrial anchor distal end configured to extend radially outward from the valve body and, thus, from the atrial anchor proximal end of the atrial tissue anchor. For example, atrial anchoring arms 2440 (i.e., the exemplary atrial tissue anchors) illustrated in FIGS. 2A and 3A may include a proximal arm end 3020 connected to annular valve body 2020 (e.g., at arm attachment junction 3202) and a distal arm end 2444 (i.e., an exemplary atrial anchor distal end) configured to extend radially outward from the annular valve body 2020 and from the proximal arm end 3020.

In some embodiments, at least one atrial tissue anchor may include a proximal anchor portion, an intermediate anchor portion, and a distal anchor portion. For example, FIG. 3B illustrates an atrial anchoring arm 2440 (i.e., an exemplary atrial tissue anchor) having a proximal arm portion 3502, an intermediate arm portion 3504, and a distal arm portion 3506. In some embodiments, the proximal arm portion 3502 may be configured to extend in an atrial direction from arm attachment junction 3202 (not depicted in FIG. 3B). Arm attachment junctions may be the locations at which atrial anchoring arms 2440 (i.e., the exemplary atrial tissue anchors) attach to the annular valve body 2020 (i.e., the exemplary valve body). In some embodiments, and as illustrated in FIG. 3B, the entire length of proximal arm portion 3502 may be configured to extend in an atrial direction (i.e., in an upward direction in FIG. 3B). Atrial anchoring arm 2440 may include a bend at a transition between proximal arm portion 3502 and intermediate arm portion 3504. As a result, in some embodiments, intermediate arm portion 3504 may be configured to extend in a ventricular direction (i.e., in a downward direction in FIG. 3B). In some alternative embodiments, the intermediate arm portion 3504 may be configured to extend laterally such that the intermediate arm portion 3504 does not extend in an atrial direction or in a ventricular direction. Atrial anchoring arm 2440 may include a second bend at the transition between intermediate arm portion 3504 and distal arm portion 3506. As a result, in some embodiments, distal arm portion 3506 may be configured to extend in an atrial direction. In some embodiments, a width of the proximal arm portion 3502 may be substantially equal to the width of at least a portion of the intermediate arm portion 3504 (the width being a dimension of the atrial anchoring arm that is perpendicular to the longitudinal axis of the valve body). Additionally, or alternatively, and as illustrated in FIG. 3B, a radially outer end of the intermediate arm portion 3504 (that is, the end of intermediate arm portion 3504 furthest from the annular valve body 2020) may have a larger width than a radially inner end of the intermediate arm portion 3504. Additionally, or alternatively, and as illustrated in FIG. 3B, distal arm portion 3506 may have a larger width than proximal arm portion 3502.

In some embodiments, the atrial tissue anchors and ventricular tissue anchors may be configured to minimize or prevent migration of the prosthetic valve into an adjacent heart chamber after the prosthetic valve is implanted within or near a native heart valve. This may be due, at least in part, to the diameter of the atrial tissue anchors and/or the ventricular tissue anchors when they are radially-expanded. That is, the atrial tissue anchors and/or the ventricular tissue anchors may form a diameter, when in the radially-expanded configuration, that is larger than the diameter of the heart valve orifice; accordingly, the prosthetic valve may be prevented from axial migration (that is, migration towards the atrium or ventricle) due to the inability of the atrial tissue anchors and/or the ventricular tissue anchors to pass through the valve orifice. Additionally, or alternatively, the atrial tissue anchors and ventricular tissue anchors may be configured to grasp or clamp tissue of the native valve to further anchor the prosthetic valve in place. For example, in the embodiment of FIGS. 10G and 10H, atrial anchoring arms 2440 (i.e., the exemplary atrial tissue anchors) may clamp tissue by exerting a ventricularly-directed force (that is, a force directed downwards towards ventricle 9020 in FIGS. 10G and 10H) on the heart valve tissue. Similarly, ventricular anchoring legs 2240 (i.e., the exemplary ventricular tissue anchors) may clamp the tissue by exerting an atrially-directed force (that is, a force directed upwards towards atrium 9010 in FIGS. 10G and 10H) on the heart valve tissue. These opposing forces may clamp or “sandwich” the heart valve tissue between the atrial tissue anchors and ventricular tissue anchors, thus firmly anchoring the prosthetic valve within the native valve.

In some embodiments, the atrial tissue anchors and ventricular tissue anchors may be constructed of one or more materials, such as a polymer or metal. The one or more materials may be biocompatible and, in some embodiments, may have shape-memory and superelastic properties. For example, the atrial tissue anchors and ventricular tissue anchors may be constructed at least partially of Nitinol, stainless steel, chromium alloys, or another other suitable material. In some embodiments, the valve body, plurality of atrial tissue anchors, and plurality of ventricular tissue anchors may be constructed substantially of the same material (e.g. Nitinol).

In some embodiments, each atrial tissue anchor may include a rigid portion situated within a radially inner portion of the atrial tissue anchor. In some embodiments, the rigid portion may extend between the proximal end of the atrial tissue anchor and a midpoint of the atrial tissue anchor. For example, in FIG. 3B, inflexible portion 3402 may constitute the rigid portion. Inflexible portion 3402 may include at least a portion of the proximal arm portion 3502 and at least a portion of the intermediate arm portion 3504; for example, the inflexible portion 3402 may extend to, and may optionally include, the proximal arm end 3020. In some embodiments, the rigid portion may be configured with a sufficiently large cross-sectional area, such that the rigid portion may be substantially rigid and inflexible. For example, the inflexible portion 3402 illustrated in FIG. 3B may be configured with a sufficiently large cross-sectional area 3402 c, such that the inflexible portion 3402 is substantially rigid and inflexible.

Additionally, or alternatively, each atrial tissue anchor may include a flexible portion situated within a radially outer portion of the atrial tissue anchor. In some embodiments, the flexible portion may be situated at a location radially external to the rigid portion, such as a position between the distal end of the rigid portion and the atrial anchor distal end. In some embodiments, the flexible portion may include a proximal end and a distal end, the distal end configured to be situated radially external to the proximal end. For example, in some embodiments, the proximal end of the flexible portion may be situated immediately adjacent to the distal end of the rigid portion of the atrial tissue anchor. The flexible portion may be configured for greater flexibility than the rigid portion. For example, in FIG. 3B, serpentine structure 3406 may constitute the flexible portion. Serpentine structure 3406 may include at least a portion of the intermediate arm portion 3504 and at least a portion of the distal arm portion 3506. In some embodiments, flexibility of the flexible portions of the atrial tissue anchors may be imparted through a structure having multiple curves, the structure having multiple curves being configured to render the flexible portion substantially flexible. The ventricular tissue anchors and the rigid portions of the atrial tissue anchors may be devoid of the structure having multiple curves, thus rendering the flexible portions of the atrial tissue anchors more flexible than the ventricular tissue anchors and the rigid portions of the atrial tissue anchors. For example, in some embodiments, the structure having multiple curves may include a serpentine pattern, such as serpentine structure 3406 illustrated in FIG. 3B. The structure having multiple curves (e.g., serpentine structure 3406) may include a thin section of the atrial tissue anchor configured to curve back and forth in a zig-zagging arrangement. This configuration may render the serpentine structure 3406 flexible and elastic (in particular, more flexible and elastic than the inflexible portion 3402 (i.e., the exemplary rigid portion) of the atrial tissue anchor). In some embodiments, the flexible portion may be less resistive to applied forces, compared to the rigid portion, due at least in part to the thin cross-section and the zig-zagging arrangement of the structure having multiple curves. However, the flexible portion may be constructed of a superelastic material such as Nitinol; as a result, the flexible portion may be configured to resist being deformed or damaged by the forces applied to the flexible portion by the native valve tissue.

In some embodiments, the rigid portion may be situated immediately adjacent to, and radially inward from, the flexible portion, along the length of the atrial tissue anchor. For example, in FIG. 3B, location 3402 d may be the transition between inflexible portion 3402 (i.e., the exemplary rigid portion) and serpentine structure 3406 (i.e., the exemplary flexible portion). Accordingly, the flexibility of the atrial anchoring arm 2440 (i.e., an exemplary atrial tissue anchor) may vary at 3402 d, because serpentine structure 3406 may be configured for greater flexibility than inflexible portion 3402.

In some embodiments, the ventricular anchor distal end of at least one ventricular tissue anchor and the distal end of the rigid portion of at least one atrial tissue anchor may be configured to be equidistant from the longitudinal axis of the valve body. That is, the distal end of the rigid portion of the at least one atrial tissue anchor may be configured to be situated at the same radial position as the terminal end of the at least one ventricular tissue anchor, relative to the longitudinal axis of the valve body. As a result, in some embodiments, the proximal end of the flexible portion of the atrial tissue anchor may be configured to be situated radially external to the distal end of the ventricular tissue anchor, since the flexible portion of the atrial tissue anchor may be situated radially external to the rigid portion of the atrial tissue anchor. For example, in some embodiments, the proximal end of the flexible portion of the at least one atrial tissue anchor may be configured to be situated radially external to the ventricular anchor distal ends of the plurality of ventricular tissue anchors. For example, the distal ends 3402 d of the inflexible portions 3402 (i.e., the exemplary rigid portions, as depicted in FIG. 3B) and the terminal leg ends 2244 (i.e., exemplary ventricular anchor distal ends) of the ventricular anchoring legs may be configured to be substantially equidistant from the center of the annular valve body 2020 (i.e., from longitudinal axis 2800 of FIGS. 2A and 2D) when the prosthetic valve is in a radially-expanded configuration. As a result, in some embodiments, the distal end of the ventricular tissue anchor and the distal end of the rigid portion of the atrial tissue anchor may be situated at the same radial position, or at similar radial positions, when the prosthetic valve is implanted.

Advantageously, in some embodiments, the arrangement of the distal end of the ventricular tissue anchor and the distal end of the rigid portion of the atrial tissue anchor may enable the ventricular tissue anchor and the rigid portion of the atrial tissue anchor to exert opposing forces on the native valve tissue, firmly grasping the tissue between the ventricular and atrial tissue anchors. For example, the ventricular tissue anchors may engage the ventricular side of a native heart valve, and may exert an atrially-directed force (that is, a force directed upwards towards the atrium) on the heart valve tissue. In addition, the atrial tissue anchors may engage the atrial side of native valve tissue; thus, the rigid portions (e.g., inflexible portions 3402 depicted in FIG. 3B) may exert a ventricularly-directed force (that is, a force directed downwards toward the ventricle) on the heart valve tissue. An example of this configuration is illustrated in FIGS. 10G and 10H, which depict atrial anchoring arms 2440 (i.e., the exemplary atrial tissue anchors) and ventricular anchoring legs 2240 (i.e., the exemplary ventricular tissue anchors) engaging atrial tissue and ventricular tissue, respectively, of mitral valve 9030, so as to clamp the mitral valve tissue between them. In particular, the placement of the structures exerting the opposing forces (i.e., the ventricular tissue anchors and the rigid portions of the atrial tissue anchors) at the same radial position may strengthen the clamping force, as the atrially-directed force and ventricularly-directed force may directly oppose one another; the clamped tissue may be securely retained between the ventricular tissue anchors and the rigid portions of the atrial tissue anchors and prevented from slipping out from between the atrial and ventricular tissue anchors. As a result, the ventricular tissue anchors and the rigid portions of the atrial tissue anchors may firmly anchor the prosthetic heart valve within the native heart valve.

In addition, including a flexible portion (such as serpentine structure 3406) in each atrial tissue anchor may increase the stability of the prosthetic valve within the native valve and further secure the prosthetic valve against axial migration. For example, the flexibility of the flexible portion may enable the flexible portion to be deformed, both laterally and axially, until the flexible portion conforms to the anatomy of the native valve. By conforming to the native valve anatomy, the flexible portion may increase the surface area of native valve tissue that is engaged by the atrial tissue anchors, stabilizing the prosthetic valve against movement relative to the native valve tissue and further securing the prosthetic valve against axial migration. In addition, the flexibility of the flexible portion may enable the outer radial half of the atrial tissue anchors to accommodate the natural motion of the native heart valve, without the outer radial half of the atrial tissue anchors sustaining damage or injuring the native valve tissue over time. Further, because the flexible portion is positioned in a section of the atrial tissue anchors external to the rigid portion, the atrial tissue anchors may be configured to exert the clamping force on tissue (via rigid portion) while also improving the stability of the prosthetic valve at the implantation site (via flexible portion).

In some embodiments, a portion of the at least one atrial tissue anchor may be configured to be substantially aligned in a common lateral plane with a portion of the at least one ventricular tissue anchor. That is, the portion of the atrial tissue anchor and the portion of the ventricular tissue anchor may be situated at the same axial position along the longitudinal axis of the valve body (e.g., longitudinal axis 2800 illustrated in FIGS. 2A and 2D). An example of such a configuration is illustrated in FIG. 2C, which depicts a ventricular anchoring leg 2240 (i.e., an exemplary ventricular tissue anchor) having a portion 2246 aligned in a common lateral plane with a portion 2446 of an atrial anchoring arm 2440 (i.e., an exemplary atrial tissue anchor), the common lateral plane being perpendicular to the longitudinal axis 2800 illustrated in FIG. 2A. That is, arm portion 2446 and leg portion 2246 may be situated at the same axial position along longitudinal axis 2800.

In some embodiments, the portion of each ventricular tissue anchor that is arranged in the common lateral plane may include the distal end of the ventricular tissue anchor; alternatively, the portion of each ventricular tissue anchor that is arranged in the common lateral plane may include a section of the ventricular tissue anchor situated radially inwards from the distal end of the ventricular tissue anchor (such as leg portion 2246 illustrated in FIG. 2C). In some embodiments, the portion of each atrial tissue anchor that is arranged in the common lateral plane (e.g., portion 2446 in FIG. 3C) may be situated in an outer radial half of the atrial tissue anchor. In some embodiments, the distal end of the rigid portion of the at least one atrial tissue anchor may be configured to be situated radially external to the portion of the atrial tissue anchor aligned in the common lateral plane. For example, as illustrated in FIG. 2C, the rigid portion distal end 3402 d may be situated radially external to (that is, to the right side of in FIG. 2C) arm portion 2446, which may be situated in the common lateral plane with leg portion 2246. As a result, in some embodiments, the entirety of the flexible portion of the at least one arm (e.g., serpentine structure 3406 illustrated in FIG. 2C), including the proximal end of the flexible portion, may be situated radially external to the arm and leg portions arranged in the common lateral plane (e.g., arm portion 2446 and leg portion 2246 in FIG. 2C). In some embodiments, the rigid portion of the at least one atrial tissue anchor may include the portion of the at least one atrial tissue anchor aligned in the common lateral plane. For example, in FIG. 2C, arm portion 2446 may be included within inflexible portion 3402 (i.e., the exemplary rigid portion) of FIG. 3B.

In some embodiments, the atrial tissue anchors and ventricular tissue anchors may be biased to assume the configuration in which the atrial tissue anchor portion and ventricular tissue anchor portion are aligned in the common lateral plane (referred to hereafter as the overlapping configuration) due at least in part to the shape-memory properties of the atrial and ventricular tissue anchors. However, upon implantation of the prosthetic valve, the prosthetic valve may grasp and retain native valve tissue between the atrial tissue anchors and ventricular tissue anchors. For example, FIGS. 10G and 10H illustrate tissue of mitral valve 9030 retained between atrial anchoring arms 2440 (i.e., the exemplary atrial tissue anchors) and ventricular anchoring legs 2240 (i.e., the exemplary ventricular tissue anchors). The retained tissue may slightly deform the atrial tissue anchors and ventricular tissue anchors, pushing the atrial and ventricular tissue anchors axially apart from each other and out of the overlapping configuration. However, due to their shape memory characteristics, the atrial tissue anchors and ventricular tissue anchors may resist the deformation and exert respective clamping forces on the retained tissue. For example, the atrial tissue anchors may clamp tissue by exerting a ventricularly-directed force (that is, a force directed downwards towards the ventricle) on the tissue. Similarly, the ventricular tissue anchors may clamp the tissue by exerting an atrially-directed force (that is, a force directed upwards towards the atrium) on the tissue. The opposing forces exerted by the rigid portions of the atrial tissue anchors and ventricular tissue anchors may clamp or “sandwich” the heart valve tissue between the atrial tissue anchors and ventricular tissue anchors, thus firmly anchoring prosthetic heart valve 6000 against axial and lateral movement within the native heart valve.

In some embodiments, the flexible portion of the at least one atrial tissue anchor may include a first segment configured to extend in a ventricular direction. Additionally, or alternatively, the flexible portion of the at least one atrial tissue anchor may include a second segment configured to extend in an atrial direction, the second segment of the flexible portion configured to be situated radially external to the first segment of the flexible portion. In the example illustrated in FIG. 3B, serpentine structure 3406 (i.e., the exemplary flexible portion) of atrial anchoring arm 2440 may include a portion of intermediate arm portion 3504 and a portion of distal arm portion 3506. Intermediate arm portion 3504 may be configured to extend in a ventricular direction (i.e., in a downward direction in FIG. 3B). Atrial anchoring arm 2440 may include a bend at the transition between intermediate arm portion 3504 and distal arm portion 3506. As a result, in some embodiments, distal arm portion 3506 may be configured to extend in an atrial direction. Distal arm portion 3506 may be situated radially external to intermediate arm portion 3504 when the atrial anchoring arm 2440 is in a radially-expanded configuration.

In some embodiments, the entire length of the at least one ventricular tissue anchor may be configured to extend radially outward in an atrial direction. The entire length of the at least one ventricular tissue anchor may refer to the tissue anchor portions extending between, and including, the ventricular anchor proximal end and the ventricular anchor distal end. In some embodiments, the entire length of the at least one ventricular tissue anchor may be configured to extend radially outward in an atrial direction when the ventricular tissue anchor is in a radially-expanded configuration. For example, as depicted in FIGS. 3C and 5E, the entire length of ventricular anchoring leg 2240 (including proximal leg end 3622 and terminal leg end 2244) extends radially outward from annular valve body 2020 (in particular, from leg attachment junction 3802) in an atrial direction when the ventricular anchoring leg is in the radially-expanded configuration.

In some embodiments, the at least one ventricular tissue anchor may include at least one opening, including a first opening. In some embodiments, the first opening may be situated within a distal portion of the at least one ventricular tissue anchor and may, in some embodiments, extend to the ventricular anchor distal end. For example, FIGS. 3C and 3D illustrate ventricular anchoring legs 2240 (i.e., the exemplary ventricular tissue anchors) having an opening 2242 in their respective distal portions. Openings 2242 may extend to the distal leg ends 2244 (i.e., exemplary ventricular anchor distal ends) of the ventricular anchoring legs 2240. In some embodiments, the first opening of the at least one ventricular tissue anchor may be situated within the widest portion of the at least one ventricular tissue anchor. For example, in FIG. 3D, the width of the ventricular anchoring leg 2240 may be larger in the distal portion encompassing opening 2242 than in portions of the ventricular anchoring leg 2240 proximal to the opening 2242.

In some embodiments, the increased width at the distal end of the at least one ventricular tissue anchor, where the first opening may be situated, may permit the ventricular tissue anchor to grasp a larger amount of native valve tissue when the prosthetic valve is implanted, thus anchoring the prosthetic valve more firmly within the native valve. In addition, the widened distal end of the at least one ventricular tissue anchor may exert lower force on native valve tissue, due to the increased area of the ventricular tissue anchor exerting force on the native valve tissue. In some embodiments, the at least one ventricular tissue anchor may have a substantially constant width between the location of attachment with the valve body and the proximal end of the first opening. For example, in FIG. 3C, ventricular anchoring legs 2240 may have a substantially constant width between leg attachment junction 3802 and the proximal (i.e., radially inner) end of opening 2242.

In some embodiments, the rigid portion of the at least one atrial tissue anchor may include a second opening. In some embodiments, the second opening may be situated within a distal portion of the rigid portion of the at least one atrial tissue anchor and may, in some embodiments, extend to the distal end of the rigid portion. For example, in FIG. 3B, inflexible portion 3402 (i.e., the exemplary rigid portion) may include an opening 2441 at or near the distal end of the inflexible portion. Opening 2441 may be situated radially inwards from (that is, proximal to) the serpentine structure 3406 (i.e., the exemplary flexible portion). In some embodiments, the second opening may be situated within the widest portion of the rigid portion of the at least one atrial tissue anchor. For example, in FIG. 2B, atrial anchoring arm 2440 (i.e., an exemplary atrial tissue anchor) may have a larger width at opening 2441 than at portions of the atrial anchoring arm radially inward from opening 2441.

In some embodiments, the increased width at the second opening of the inflexible portion of the atrial tissue anchor may improve the ability of the inflexible portion to grasp native valve tissue when the prosthetic valve is implanted. For example, when the ventricular tissue anchors and the rigid portions of the atrial tissue anchors exert their respective clamping forces on native valve tissue (as discussed above), the widened width of the atrial tissue anchors at the second openings may permit the distal ends of the rigid portions of the atrial tissue anchors to grasp a larger amount of native valve tissue. As a result, the rigid portions may more securely retain native valve tissue between the atrial tissue anchors and ventricular tissue anchors, permitting the rigid portions and the ventricular tissue anchors to clamp native valve tissue without the tissue sliding out from between the atrial tissue anchors and ventricular tissue anchors.

In some embodiments, the first opening of the ventricular tissue anchor and the second opening of the atrial tissue anchor may be configured to be equidistant from the longitudinal axis of the valve body (i.e., from the center of the valve body). In some embodiments, the first and second openings may be equidistant from the longitudinal axis of the valve body when the prosthetic valve is in the radially-expanded configuration (e.g., the configuration illustrated in FIG. 5E). For example, in the embodiment depicted in FIG. 2B, openings 2441 and openings 2242 may be substantially equidistant from the longitudinal axis 2800 of the annular valve body 2020 (that is, from the center of annular valve body 2020). Additionally, or alternatively, the first and second openings may be equidistant from the longitudinal axis of the valve body when the atrial tissue anchors and ventricular tissue anchors are radially expanded, but the valve body remains radially contracted (e.g., the configuration illustrated in FIG. 5D). Advantageously, the first opening and second opening may exert opposing grasping forces on tissue when they are equidistant from the longitudinal axis of the valve body, thus better securing the grasped tissue between the atrial and ventricular tissue anchors.

In some embodiments, the exemplary valve body may include one or more frames. In some embodiments, the valve body may include an annular outer frame and an inner frame situated at least partially within the annular outer frame. In some embodiments, one or both of the inner frame and the outer frame may be annular, and the inner frame may be positioned within an opening of the outer frame. For example, FIG. 2A depicts an exemplary prosthetic valve frame 2000 having an outer frame 2200 and an inner frame 2400 situated at least partially within outer frame 2200. In some alternative embodiments, the inner frame may be situated entirely within the outer frame. One or both of the inner frame and the outer frame may be configured to radially expand between a radially-contracted configuration (e.g., a crimped state) and a radially-expanded configuration. In some embodiments, the inner frame may be configured to receive or otherwise support a flow control device, such as one or more leaflets, for regulating flow of blood or other bodily fluids through the prosthetic valve.

In some embodiments, the annular outer frame may include an atrial end, a ventricular end opposite of the atrial end of the outer frame, and an intermediate portion extending between the atrial end of the outer frame and the ventricular end of the outer frame. Additionally, or alternatively, the inner frame may include an atrial end, a ventricular end opposite of the atrial end of the inner frame, and an intermediate portion extending between the atrial end of the inner frame and the ventricular end of the inner frame. In some embodiments, the atrial end may refer to the portion of a feature (e.g., the outer frame) configured to be situated closest to the atrium, or at a location within the atrium that is furthest from an adjacent ventricle, when the exemplary prosthetic valve is implanted in a native heart valve. Additionally, or alternatively, the ventricular end may refer to the portion of a feature configured to be situated closest to the ventricle, or at a location within the ventricle that is furthest from an adjacent atrium, when the exemplary prosthetic valve is implanted in a native heart valve. The atrial end and ventricular end of a given feature may form opposite ends of that feature. For example, as depicted in FIGS. 2A and 3C, atrial end outer frame junctions 3602 and ventricular end outer frame junctions 3604 may constitute the atrial end and ventricular end, respectively, of outer frame 2200. In addition, and as depicted in FIGS. 2A and 3A, atrial end inner frame junctions 3002 and ventricular end inner frame junctions 3004 may constitute the atrial end and ventricular end, respectively, of inner frame 2400.

In some embodiments, the intermediate portion of a feature (e.g., outer frame 2200) may include every portion of the feature situated in between the atrial end and ventricular end of that feature. For example, as depicted in FIG. 3C, the intermediate portion 3606 of the outer frame may include every portion of the outer frame 2200 positioned between the atrial end outer frame junctions 3602 and ventricular end outer frame junctions 3604. In addition, and as depicted in FIG. 3A, the intermediate portion 3006 of the inner frame may include every portion of the inner frame 2400 positioned between the atrial end inner frame junctions 3002 and ventricular end inner frame junctions 3004.

In some embodiments, the ventricular tissue anchors may extend from the intermediate portion of the outer frame. For example, as illustrated in FIG. 3C, leg attachment junctions 3802 (from which ventricular anchoring legs 2240 extend) are situated in the intermediate portion 3606 of the outer frame 2200, and are accordingly spaced apart from the atrial end and ventricular end of the outer frame. Additionally, or alternatively, the atrial tissue anchors may extend from the intermediate portion of the inner frame. For example, as illustrated in FIG. 3A, arm attachment junctions 3202 (from which atrial anchoring arms 2440 extend) are situated in the intermediate portion 3006 of the inner frame 2400, and are accordingly spaced apart from the atrial end and ventricular end of the inner frame.

In some embodiments, the atrial tissue anchors may be angularly offset from at least one location of connection between the outer frame and inner frame. In some embodiments, the inner and outer frames may be connected by pins, screws, welding, soldering, adhesive, magnets, and/or any other suitable mechanism. The inner and outer frames may be secured together at multiple points of the inner frame and outer frame. For example, FIG. 2A depicts inner frame 2400 and outer frame 2200 connected by a plurality of connector pins 2040, each situated at a different circumferential position of the valve frame 2000 and each configured to extend between the inner frame 2400 and outer frame 2200 to secure them together. In the example of FIG. 2A, inner frame 2400 and outer frame 2200 may be connected together by twelve connector pins 2040. Alternatively, any suitable number of connector pins may be utilized to secure the inner and outer frames together. As illustrated in FIG. 2A, atrial anchoring arms 2440 (i.e., the exemplary atrial tissue anchors) may be angularly offset from connector pins 2040. That is, atrial anchoring arms 2440 and connector pins 2040 may be positioned at different positions about the circumference of annular valve body 2020 (i.e., the exemplary valve body).

In some embodiments, and as explained above, each atrial tissue anchor may include a rigid portion (e.g., inflexible portion 3402) and a flexible portion (e.g., serpentine structure 3406). Additionally, or alternatively, each ventricular tissue anchor may be devoid of structures configured to render the ventricular tissue anchors flexible, including serpentine structure 3406 (i.e., the exemplary flexible portion). As a result, the plurality of atrial tissue anchors and the plurality of ventricular tissue anchors may be arranged in a symmetrical fashion about the valve body, because each atrial tissue anchor may be identically configured and each ventricular tissue anchor may be identically configured. As a result, the expandable valve body may be configured to be implanted in a native valve independent of the rotational position of the atrial tissue anchors and ventricular tissue anchors relative to the native valve. That is, because the atrial tissue anchors and ventricular tissue anchors may be symmetrically arranged, the atrial tissue anchors and ventricular tissue anchors may be configured to grasp the native valve tissue and anchor the prosthetic valve within the native valve against axial migration (as discussed above), at any rotational relationship between the prosthetic valve and the native valve. Advantageously, this may simplify the implantation process of the prosthetic valve enormously, since the prosthetic valve does not need to be implanted at any specific rotational position within the native valve.

The foregoing description has been presented for purposes of illustration. It is not exhaustive and is not limited to precise forms or embodiments disclosed. Modifications and adaptations of the embodiments will be apparent from consideration of the specification and practice of the disclosed embodiments. For example, while certain components have been described as being coupled to one another, such components may be integrated with one another or distributed in any suitable fashion.

Moreover, while illustrative embodiments have been described herein, the scope includes any and all embodiments having equivalent elements, modifications, omissions, combinations (e.g., of aspects across various embodiments), adaptations and/or alterations based on the present disclosure. The elements in the claims are to be interpreted broadly based on the language employed in the claims and not limited to examples described in the present specification or during the prosecution of the application, which examples are to be construed as nonexclusive. Further, the steps of the disclosed methods can be modified in any manner, including reordering steps and/or inserting or deleting steps.

The features and advantages of the disclosure are apparent from the detailed specification, and thus, it is intended that the appended claims cover all systems and methods falling within the true spirit and scope of the disclosure. As used herein, the indefinite articles “a” and “an” mean “one or more.” Similarly, the use of a plural term does not necessarily denote a plurality unless it is unambiguous in the given context. Words such as “and” or “or” mean “and/or” unless specifically directed otherwise. Further, since numerous modifications and variations will readily occur from studying the present disclosure, it is not desired to limit the disclosure to the exact construction and operation illustrated and described, and, accordingly, all suitable modifications and equivalents may be resorted to, falling within the scope of the disclosure.

Other embodiments will be apparent from consideration of the specification and practice of the embodiments disclosed herein. It is intended that the specification and examples be considered as example only, with a true scope and spirit of the disclosed embodiments being indicated by the following claims. 

What is claimed is:
 1. A prosthetic valve configured for implantation within a native valve, the prosthetic valve comprising: an expandable valve body having an inner lumen extending along a longitudinal axis of the valve body; a plurality of ventricular tissue anchors configured to extend radially outward from the valve body to respective ventricular anchor distal ends; and a plurality of atrial tissue anchors configured to extend radially outward from the valve body to respective atrial anchor distal ends, each atrial tissue anchor including: a rigid portion, and a flexible portion situated between a distal end of the rigid portion and the atrial anchor distal end, wherein flexibility of the flexible portion of each atrial tissue anchor is imparted through a structure having multiple curves, wherein the ventricular anchor distal end of at least one ventricular tissue anchor and the distal end of the rigid portion of at least one atrial tissue anchor are configured to be equidistant from the longitudinal axis of the valve body, and wherein the ventricular tissue anchors and the rigid portions of the atrial tissue anchors are devoid of the structure having multiple curves.
 2. The prosthetic valve of claim 1, wherein a portion of the at least one atrial tissue anchor is configured to be aligned in a common lateral plane with a portion of the at least one ventricular tissue anchor.
 3. The prosthetic valve of claim 2, wherein the distal end of the rigid portion of the at least one atrial tissue anchor is configured to be situated radially external to the portion of the at least one atrial tissue anchor aligned in the common lateral plane.
 4. The prosthetic valve of claim 1, wherein the flexible portion of the at least one atrial tissue anchor includes: a first segment configured to extend in a ventricular direction, and a second segment configured to extend in an atrial direction, the second segment of the flexible portion configured to be situated radially external to the first segment of the flexible portion.
 5. The prosthetic valve of claim 1, wherein an entire length of the at least one ventricular tissue anchor is configured to extend radially outward in an atrial direction.
 6. The prosthetic valve of claim 1, wherein the ventricular anchor distal end of the at least one ventricular tissue anchor and the distal end of the rigid portion of the at least one atrial tissue anchor are configured to apply opposing grasping forces upon the native valve.
 7. The prosthetic valve of claim 1, wherein the at least one ventricular tissue anchor includes a first opening, the first opening situated within the widest portion of the at least one ventricular tissue anchor; wherein the rigid portion of the at least one atrial tissue anchor includes a second opening, the second opening situated within the widest portion of the rigid portion of the at least one atrial tissue anchor; and wherein the first opening and second opening are configured to be equidistant from the longitudinal axis of the valve body.
 8. The prosthetic valve of claim 1, wherein the valve body comprises: an annular outer frame having an atrial end, a ventricular end opposite of the atrial end of the outer frame, and an intermediate portion extending between the atrial end of the outer frame and the ventricular end of the outer frame; and an inner frame situated at least partially within the outer frame, the inner frame having an atrial end, a ventricular end opposite of the atrial end of the inner frame, and an intermediate portion extending between the atrial end of the inner frame and the ventricular end of the inner frame, wherein the ventricular tissue anchors extend from the intermediate portion of the outer frame and the atrial tissue anchors extend from the intermediate portion of the inner frame.
 9. The prosthetic valve of claim 8, wherein the atrial tissue anchors are angularly offset from at least one location of connection between the outer frame and inner frame.
 10. A prosthetic valve configured for implantation within a native valve, the prosthetic valve comprising: an expandable valve body; a plurality of ventricular tissue anchors configured to extend radially outward from the valve body to respective ventricular anchor distal ends; and a plurality of atrial tissue anchors configured to extend radially outward from the valve body, each atrial tissue anchor including: a rigid portion, and a flexible portion having a proximal end and a distal end configured to be situated radially external to the proximal end, flexibility of the flexible portion of each atrial tissue anchor being imparted through a structure having multiple curves, wherein the proximal end of the flexible portion is immediately adjacent to the rigid portion, wherein the proximal end of the flexible portion of at least one atrial tissue anchor is configured to be situated radially external to the ventricular anchor distal ends of the plurality of ventricular tissue anchors, and wherein the ventricular tissue anchors and the rigid portions of the atrial tissue anchors are devoid of the structure having multiple curves.
 11. The prosthetic valve of claim 10, wherein a portion of the at least one atrial tissue anchor is configured to be aligned in a common lateral plane with a portion of at least one ventricular tissue anchor.
 12. The prosthetic valve of claim 11, wherein the proximal end of the flexible portion of the at least one atrial tissue anchor is configured to be situated radially external to the portion of the at least one atrial tissue anchor aligned in the common lateral plane.
 13. The prosthetic valve of claim 11, wherein the rigid portion of the at least one atrial tissue anchor includes the portion of the at least one atrial tissue anchor aligned in the common lateral plane.
 14. The prosthetic valve of claim 10, wherein the flexible portion of the at least one atrial tissue anchor includes: a first segment configured to extend in a ventricular direction, and a second segment configured to extend in an atrial direction, the second segment of the flexible portion configured to be situated radially external to the first segment of the flexible portion.
 15. The prosthetic valve of claim 10, wherein an entire length of at least one ventricular tissue anchor is configured to extend radially outward in an atrial direction.
 16. The prosthetic valve of claim 10, wherein the expandable valve body is configured to be implanted in the native valve independent of the rotational position of the atrial tissue anchors and ventricular tissue anchors relative to the native valve.
 17. The prosthetic valve of claim 10, wherein the valve body comprises: an annular outer frame having an atrial end, a ventricular end opposite of the atrial end of the outer frame, and an intermediate portion extending between the atrial end of the outer frame and the ventricular end of the outer frame; and an inner frame situated at least partially within the outer frame, the inner frame having an atrial end, a ventricular end opposite of the atrial end of the inner frame, and an intermediate portion extending between the atrial end of the inner frame and the ventricular end of the inner frame, wherein the ventricular tissue anchors extend from the intermediate portion of the outer frame and the atrial tissue anchors extend from the intermediate portion of the inner frame.
 18. The prosthetic valve of claim 17, wherein the atrial tissue anchors are angularly offset from at least one location of connection between the outer frame and inner frame. 